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Alkynes: Structure, Nomenclature, Properties, and Reactions

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Alkyne Hydrohalogenation

  • Double hydrohalogenation of alkynes.
    02:20
  • General properties of double addition reactions to alkynes.
    01:01

Alkyne Halogenation

  • Double halogenation of alkynes.
    02:15

Alkyne Hydration

  • Vinyl alcohols yield tautomers.
    03:51
  • Markovnikov addition of alcohols yields ketones.
    03:29

Alkyne Hydroboration

  • Anti-Markovnikov addition of alcohols to terminal alkynes yields aldehydes
    02:43

Alkyne Halogenation

  • Double halogenation of alkynes.
    02:15

Acidity of Aromatic Hydrocarbons

  • Aromatic hydrocarbon acidity
    05:39
  • Comparing hydrocarbon acidity
    02:41
  • Determining hydrocarbon acitidy
    01:50

Hybridization

  • How carbon creates 4 partially-filled orbitals.
    02:53
  • Bond sites, hybridization, and intermediate orbitals
    04:58
  • Introduction to the reactive intermediates.
    02:47

Alkane Nomenclature

  • Naming the root chain
    01:02
  • Provide the IUPAC name for the following alkane
    07:08
  • The different parts of an IUPAC name
    03:43

Addition Reaction

  • Provide the mechanism
    01:15
  • Features of Addition Mechanisms.
    05:39

Tautomerization

  • Tautomerization Mechanisms
    05:11
  • Unusual Acidity of the Alpha Carbon
    01:51

Ozonolysis

  • General properties of ozonolysis.
    06:30

Oxidative Cleavage

  • General properties of strong oxidative cleavage.
    06:00